Use of QRX3 for Acute Tubular Necrosis Type of Renal Failure in Hospitalized Patients ( QRX-3 in ARF)

Trial statusNot yet recruiting
Trial phasePhase 2, Phase 3
Trial typeInterventional
Biological sexAll
Age10-80
SponsorEbima Clifford Okundaye

About this trial

Use of QRX-3 in hospitalized patients with pediatric and adult patients with acute tubular necrosis renal failure

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Hospitalized patients

presence of Acute renal failure

Nephrologist diagnosis of Acute tubular necrosis or fractional excretion of sodium of >2%

willingness to participate

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • QRX-3

    Drug

    Combination of QRX-3 with standard therapy will be given to one arm in trial , another arm will receive placebo

Treatment groups

500 Participants
are divided into 2 treatment groups
Group A: Use of QRX-3 in addition to standard therapyExperimental treatment 1 intervention
Group B: control groupPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Rate of change in creatinine glomerular filtration rate

compare the outcome effect of added QRX-3 drug to placebo in addition to standard therapy on the rate of change from baseline of creatinine GFR in ATN patients

Time frame
28 days

Secondary outcomes

1

daily change in glomerular filtration rate in ml/min

daily change in GFR by creatinine in mls/min

Time frame
7 days
2

daily change in cystatin C level in mg/dl

daily change in measured cystatin C level

Time frame
7 days

Other outcomes

1

effect of QRX-3 on recovery of renal function in patients with ATN renal failure

comparism of number of patient achieving return to baseline renal function in both groups

Time frame
28

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Ebima Clifford Okundaye

Lead sponsor

Neukidney Inc.

Sponsor institution

This trial is not recruiting at the moment. You can still explore other options: